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Detection of Urogenital Mycoplasmas Using Culture and PCR: A Descriptive Pilot Study

机译:使用培养和PCR检测泌尿生殖道支原体:描述性试验研究

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Mycoplasmas as human urogenital tract pathogens are associated with infections, reproductive failures and adverse pregnancy outcomes and thus very important to diagnose. Several methods have been used to detect genitourinary Mycoplasmas, each having their own limitations, advantages and disadvantages. In the present study, researchers used microbial culture and PCR to detect Mycoplasmas in urogenital specimens with the aim of comparing detection rate, sensitivity and specificity of the two methods. It was a descriptive cross sectional pilot study. About 30 urogenital samples including 17 vaginal swabs, 7 male urine and 6 female urine samples were collected from patients referring to hospitals regardless of their disease and studied for Mycoplasmas by culture (using two media: PPLO agar and PPLO broth) and PCR. Of total 30 specimens, Mycoplasmas were detected in 14, 11 and 11 of them using PPLO broth culture medium, PPLO agar culture medium and PCR, respectively. Accordingly, the specificity and specificity of the PCR Method was determined 100 and 95%, respectively while culture was found to have a sensitivity of 77% and specificity of 66%. Researchers found PCR based on 16S rRNA sequences to be highly sensitive and specific offering a rapid, easy and cost benefit method for detection of Mycoplasmas in comparison to Microbial Culture Method.
机译:支原体作为人的泌尿生殖道病原体与感染,生殖衰竭和不良妊娠结局有关,因此对诊断非常重要。已经使用了几种方法来检测生殖泌尿道支原体,每种方法都有其自身的局限性,优点和缺点。在本研究中,研究人员使用微生物培养和PCR检测泌尿生殖道标本中的支原体,以比较两种方法的检测率,敏感性和特异性。这是一个描述性的横断面试验研究。不论病情如何,均从转诊医院的患者那里收集了大约30个泌尿生殖道标本,包括17个阴道拭子,7个男性尿液和6个女性尿液样本,并通过培养(使用两种培养基:PPLO琼脂和PPLO肉汤)和PCR研究了支原体。在总共30个标本中,分别使用PPLO肉汤培养基,PPLO琼脂培养基和PCR检测了14、11和11个支原体。因此,测定PCR方法的特异性和特异性分别为100%和95%,而发现培养物具有77%的敏感性和66%的特异性。研究人员发现,与微生物培养法相比,基于16S rRNA序列的PCR具有高度的敏感性和特异性,为检测支原体提供了一种快速,简便且经济实惠的方法。

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